BCL-2 AND IAP Proteins As Potential Drug Targets
Author(s) -
Stephen W. Fesik
Publication year - 2001
Publication title -
the scientific world journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.453
H-Index - 93
eISSN - 2356-6140
pISSN - 1537-744X
DOI - 10.1100/tsw.2001.129
Subject(s) - drug , drug target , drug discovery , computational biology , computer science , chemistry , pharmacology , biology , biochemistry
. Members of the Bcl-2 and IAP families of proteins inhibit apoptosis and are overexpressed in many cancers. Thus, small molecules that bind to these proteins and block their anti-apoptotic activity may induce cell death and be useful for the treatment of cancer. To aid in the design of these small molecules that bind to these proteins, we have determined the three-dimensional structures of Bcl-2 and IAP family members alone and when complexed to inhibitors (1-6).
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